Potassium Chloride
- Product NDC
- 50090-1994
- 11-digit product format
- 500901994
- Labeler code
- 50090
- Product ID
- 50090-1994_46da3f1b-600d-49a6-9c92-01dd613a6025
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA204662
- Marketing category
- ANDA
- Marketing start
- 2016-11-09
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 10 meq/1
- Pharmacologic classes
- Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1994-0 | 50090199400 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1994-0) | 2016-11-09 | 0000-00-00 | No | No | Current |
| 50090-1994-1 | 50090199401 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1994-1) | 2016-11-09 | 0000-00-00 | No | No | Current |
| 50090-1994-2 | 50090199402 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1994-2) | 2016-11-09 | 0000-00-00 | No | No | Current |
| 50090-1994-3 | 50090199403 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1994-3) | 2016-11-09 | 0000-00-00 | No | No | Current |